Safety and efficacy of phosphodiesterase-5 (PDE-5) inhibitors in fetal growth restriction: a systematic literature review and meta-analysis.

IF 2.9 4区 医学 Q2 PHARMACOLOGY & PHARMACY Journal of Pharmacy and Pharmaceutical Sciences Pub Date : 2024-08-15 eCollection Date: 2024-01-01 DOI:10.3389/jpps.2024.13206
Ying Liu, Ella Man-Wai Un, Ying Bai, Man Keong Chan, Luo Xin Zeng, Sut Leng Lei, Junjun Li, Carolina Oi Lam Ung
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Abstract

Introduction: Fetal growth restriction (FGR) is associated with a higher risk of perinatal morbidity and mortality, as well as long-term health issues in newborns. Currently, there is no effective medicine for FGR. Phosphodiesterase-5 (PDE-5) inhibitors have been shown in pre-clinical studies to improve FGR. This study aimed to evaluate the latest evidence about the clinical outcomes and safety of PDE-5 inhibitors for the management of FGR. Methods: Eight databases (PubMed, Embase, Medline, Web of Science, Cochrane Library, Chinese National Knowledge Infrastructure, Chinese Biomedical Database and WangFang Database) were searched for English and Chinese articles published from the database inception to December 2023. Randomized controlled trials (RCTs) reporting the use of PDE-5 inhibitors in FGR were included. The quality of the RCTs was assessed using the Cochrane Risk of Bias Tool. Odds ratio and mean difference (MD) (95% confidence intervals) were pooled for meta-analysis. Results: From 253 retrieved publications, 16 studies involving 1,492 pregnant women met the inclusion criteria. Only sildenafil (15 RCTs) and tadalafil (1 RCT) were studied for FGR. Compared with the control group (placebo, no treatment, or other medication therapies), sildenafil increased birth weight, pregnancy prolongation and umbilical artery pulsatility indices. However, it also increased the risk of pulmonary hypertension in newborns, as well as headache and flushing/rash in mothers. There were no significant differences in gestation age, perinatal mortality or major neonatal morbidity, stillbirth, neonate death, infants admitted to neonatal intensive care unit, intraventricular hemorrhage and necrotizing enterocolitis in infants, as well as pregnancy hypertension and gastrointestinal side effects in mothers between the treatment and the control groups. Discussion: Sildenafil was the most investigated PDE-5 inhibitors for FGR. Current evidence suggests that sildenafil can improve birth weight and duration of pregnancy but at the same time increase the risk of neonatal pulmonary hypertension. It remains uncertain whether the benefits of sildenafil in FGR outweigh the risks and further high-quality RCTs are warranted. Systematic Review Registration: https://www.crd.york.ac.uk/prospero/display_record.php?RecordID=325909.

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磷酸二酯酶-5(PDE-5)抑制剂对胎儿生长受限的安全性和有效性:系统文献综述和荟萃分析。
导言:胎儿生长受限(FGR)与围产期发病率和死亡率较高以及新生儿长期健康问题有关。目前,尚无治疗 FGR 的有效药物。临床前研究显示,磷酸二酯酶-5(PDE-5)抑制剂可改善FGR。本研究旨在评估有关 PDE-5 抑制剂治疗 FGR 的临床效果和安全性的最新证据。方法:在八个数据库(PubMed、Embase、Medline、Web of Science、Cochrane Library、中国国家知识基础设施、中国生物医学数据库和王方数据库)中检索了自数据库建立至 2023 年 12 月期间发表的中英文文章。纳入的随机对照试验(RCT)报告了PDE-5抑制剂在FGR中的应用。采用 Cochrane 偏倚风险工具评估 RCT 的质量。对比值比和平均差 (MD) (95% 置信区间)进行汇总,以进行荟萃分析。结果在检索到的 253 篇文献中,有 16 项研究符合纳入标准,涉及 1,492 名孕妇。其中只有西地那非(15 项研究)和他达拉非(1 项研究)针对 FGR 进行了研究。与对照组(安慰剂、无治疗或其他药物疗法)相比,西地那非可增加出生体重、妊娠期延长和脐动脉搏动指数。然而,西地那非也增加了新生儿肺动脉高压的风险,以及母亲头痛和潮红/皮疹的风险。治疗组和对照组在妊娠年龄、围产期死亡率或新生儿主要发病率、死胎、新生儿死亡、新生儿重症监护室住院、婴儿脑室内出血和坏死性小肠结肠炎以及母亲妊娠高血压和胃肠道副作用方面没有明显差异。讨论西地那非是研究最多的用于治疗FGR的PDE-5抑制剂。目前的证据表明,西地那非可以改善出生体重和妊娠持续时间,但同时会增加新生儿肺动脉高压的风险。目前仍无法确定西地那非治疗 FGR 的益处是否大于风险,因此有必要进一步开展高质量的 RCT 研究。系统综述注册:https://www.crd.york.ac.uk/prospero/display_record.php?RecordID=325909。
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来源期刊
CiteScore
6.90
自引率
0.00%
发文量
29
审稿时长
6-12 weeks
期刊介绍: The Journal of Pharmacy and Pharmaceutical Sciences (JPPS) is the official journal of the Canadian Society for Pharmaceutical Sciences. JPPS is a broad-spectrum, peer-reviewed, international pharmaceutical journal circulated electronically via the World Wide Web. Subscription to JPPS is free of charge. Articles will appear individually as soon as they are accepted and are ready for circulation.
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